•Preferably a graduate of BS Chemistry, BS Pharmacy, BS Biology or any allied course
•Preferably with at least two years of working experience as a QC Analyst (or equivalent) in a pharmaceutical manufacturing industry
•Excellent in analytical testing and able to operate major analytical instruments such as HPLC, GC, UV-Vis, AAS, IR,
Dissolution Tester, etc.
•Must have a strong analytical skills with exceptional attention to details
•Familiar with Good Manufacturing Practices
•Observes Good Laboratory Practices
•With initiative; can work under pressure and with minimal supervision
•Flexible and willing to be assigned in any shift
•Willing to be assigned in Silang, Cavite
The Quality Control Analyst performs physical and chemical testing of raw materials, in-process and finished goods
following the approved methods and procedures. He/she ensures that all test results are properly documented for easy reference. He/she must always conform to guidelines and procedures set in the various standards and outlined in GLP and GMP.